CN116803364A - 具有改进的冲洗性能的用于清洁角蛋白材料的组合物 - Google Patents
具有改进的冲洗性能的用于清洁角蛋白材料的组合物 Download PDFInfo
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- CN116803364A CN116803364A CN202310893993.9A CN202310893993A CN116803364A CN 116803364 A CN116803364 A CN 116803364A CN 202310893993 A CN202310893993 A CN 202310893993A CN 116803364 A CN116803364 A CN 116803364A
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- FCBUGCHAVCFTHW-NTISSMGPSA-N sodium;(2s)-2-(tetradecanoylamino)pentanedioic acid Chemical compound [Na].CCCCCCCCCCCCCC(=O)N[C@H](C(O)=O)CCC(O)=O FCBUGCHAVCFTHW-NTISSMGPSA-N 0.000 description 1
- IEXXLSKKBWIDAC-ZOWNYOTGSA-M sodium;(3s)-3-(dodecanoylamino)-4-hydroxy-4-oxobutanoate Chemical compound [Na+].CCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CC(O)=O IEXXLSKKBWIDAC-ZOWNYOTGSA-M 0.000 description 1
- IFYJQGOKVNCMTC-RSAXXLAASA-M sodium;(3s)-4-hydroxy-4-oxo-3-(tetradecanoylamino)butanoate Chemical compound [H+].[Na+].CCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CC([O-])=O IFYJQGOKVNCMTC-RSAXXLAASA-M 0.000 description 1
- KLIFRVSZGDONER-FERBBOLQSA-M sodium;(4s)-4-(hexadecanoylamino)-5-hydroxy-5-oxopentanoate Chemical compound [H+].[Na+].CCCCCCCCCCCCCCCC(=O)N[C@H](C([O-])=O)CCC([O-])=O KLIFRVSZGDONER-FERBBOLQSA-M 0.000 description 1
- KDHFCTLPQJQDQI-BDQAORGHSA-M sodium;(4s)-4-amino-5-octadecanoyloxy-5-oxopentanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC(=O)OC(=O)[C@@H](N)CCC([O-])=O KDHFCTLPQJQDQI-BDQAORGHSA-M 0.000 description 1
- KPTLOKOTBGOYCE-PPHPATTJSA-M sodium;(4s)-4-amino-5-octanoyloxy-5-oxopentanoate Chemical compound [Na+].CCCCCCCC(=O)OC(=O)[C@@H](N)CCC([O-])=O KPTLOKOTBGOYCE-PPHPATTJSA-M 0.000 description 1
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 1
- YBDZITJALUSANZ-UHFFFAOYSA-M sodium;2-(tetradecanoylamino)acetate Chemical compound [Na+].CCCCCCCCCCCCCC(=O)NCC([O-])=O YBDZITJALUSANZ-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- LPWCRLGKYWVLHQ-UHFFFAOYSA-N tetradecanoyl chloride Chemical compound CCCCCCCCCCCCCC(Cl)=O LPWCRLGKYWVLHQ-UHFFFAOYSA-N 0.000 description 1
- HFRXJVQOXRXOPP-UHFFFAOYSA-N thionyl bromide Chemical compound BrS(Br)=O HFRXJVQOXRXOPP-UHFFFAOYSA-N 0.000 description 1
- LSJNBGSOIVSBBR-UHFFFAOYSA-N thionyl fluoride Chemical compound FS(F)=O LSJNBGSOIVSBBR-UHFFFAOYSA-N 0.000 description 1
- RKIDPTUGNXTOMU-UHFFFAOYSA-N thionyl iodide Chemical compound IS(I)=O RKIDPTUGNXTOMU-UHFFFAOYSA-N 0.000 description 1
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- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Chemical class OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004474 valine Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
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Abstract
本发明涉及用于处理角蛋白材料的组合物,其包含至少一种氨基酸表面活性剂、至少一种两性或两性离子表面活性剂、至少一种固体脂肪酸、至少一种淀粉磷酸酯和至少一种丙烯酸类增稠聚合物。所述组合物在施用后具有改进的冲洗速度,并且在2个月内稳定,具有改进的发泡性能,例如泡沫密度和发泡体积。
Description
本申请是申请日为2015年12月10日的申请号为201580085193.8的题为“具有改进的冲洗性能的用于清洁角蛋白材料的组合物”的发明专利申请的分案申请。
技术领域
本发明涉及用于清洁角蛋白材料的组合物。更特别地,本发明涉及用于清洁角蛋白材料、特别是皮肤和头皮的组合物,其具有改进的冲洗性能和发泡性能。
背景技术
清洁皮肤尤其对于护理面部是非常重要的。它必须尽可能高效,因为油脂性残留物,如污垢,过多皮脂以及每日使用的美容产品残余物和化妆品会导致令人不快的油性外观。皮肤的油性外观问题在油性皮肤上甚至更为严重。
而且,现在已变得越来越重要的是,清洁组合物提供角蛋白材料的有效清洁以及所述角蛋白材料的温和性。
已经做出努力来满足如上所述的要求。因此,更频繁地使用温和的表面活性剂,例如氨基酸表面活性剂来提供温和的、高满意度的清洁剂。例如,已知将氨基酸表面活性剂与高水平的烃蜡和油润肤剂组合配制以获得在施用后具有良好皮肤感觉的温和发泡清洁产品。
但它仍然不令人满意。
上述现有技术在油性皮肤上施用时特别不令人满意,特别是在冲洗速度方面。即使在10个冲洗循环后仍存在粘滑感,和因此不被消费者所需,特别是具有油性皮肤类型的那些。
此外,申请人发现,通过简单地减少现有技术的烃蜡和油润滑剂,难以获得具有上述美容性能并且随时间推移稳定的温和组合物。
因此,有需要配制用于处理角蛋白材料的组合物,特别是用于清洁角蛋白材料的组合物,其具有改进的冲洗速度和稳定性。
此外,有需要配制如上所述的这种组合物,其具有良好的清洁性能,例如泡沫密度。
更特别地,存在配制具有改进的发泡体积的这种组合物的需要,特别是在存在皮脂的情况下,例如在油性或油脂性皮肤上。
发明内容
申请人发现可以通过配制用于处理角蛋白材料的组合物来满足这种需要,所述组合物包含表面活性剂、固体脂肪酸、淀粉磷酸酯和丙烯酸类增稠聚合物的特定组合。
更特别地,本发明的一个方面是一种组合物,其包含:
a)至少一种氨基酸表面活性剂;
b)至少一种两性或两性离子表面活性剂;
c)至少一种固体脂肪酸;
d)至少一种淀粉磷酸酯;和
e)至少一种丙烯酸类增稠聚合物。
如上所述的组合物是用于处理角蛋白材料的组合物,特别是用于护理和/或化妆角蛋白材料的组合物。
这种组合物旨在用于清洁角蛋白材料、特别是皮肤。
更特别地,本发明的另一方面是用于处理角蛋白材料、特别是皮肤和头皮的方法,包括将根据本发明的组合物施用于角蛋白材料。
优选地,所述方法旨在用于清洁角蛋白材料。
特别地,所述方法包括在任选的一段时间后冲洗掉根据本发明的组合物。
本发明还涉及根据本发明的组合物用于清洁角蛋白材料、特别是皮肤的用途。
用“角蛋白材料”旨在表示人角蛋白材料,且更特别地是皮肤和头皮,且更特别是面部的皮肤。
“随时间推移稳定”应理解为表示本发明的组合物,其在4℃和45℃之间的所有温度下储存2个月后,在颜色、气味或粘度上不显示任何宏观变化,在pH或微观外观上不显示任何改变。
通过阅读下面的描述和实施例,本发明的其他主题和特征、方面和优点将甚至更加清楚地显现。
在接下来的内容中,除非另外指出,否则值的范围的界限被包括在该范围内,特别是在“......之间”和“......至......的范围内”的表述中。
此外,在本说明书中使用的表述“至少一种”等同于表述“一种或多种”。
发明详述
氨基酸表面活性剂
本发明的组合物包含至少一种氨基酸表面活性剂。
在一个实施方案中,所述氨基酸表面活性剂衍生自氨基酸的羧酸盐,其中位于氨基酸盐的α-碳或β-碳上的胺基用C8至C22脂肪酸衍生物酰化。
这些氨基酸的羧酸盐可以通过常规方法形成,例如通过用碱中和相应的氨基酸。位于被中和的氨基酸的α-碳或β-碳上的胺基在碱存在下经由熟知的肖特-鲍曼反应用脂肪酸卤化物(卤化酰基)酰化产生酰胺,从而形成所需的表面活性剂反应产物,即氨基酸表面活性剂。用于酰化氨基酸羧酸盐的合适卤化酰基包括氯化酰基、溴化酰基、氟化酰基和碘化酰基。卤化酰基可通过使饱和或不饱和、直链或支链的C8至C22脂肪酸与亚硫酰卤(亚硫酰溴、亚硫酰氯、亚硫酰氟和亚硫酰碘)反应来制备。代表性的卤化酰基包括但不限于选自癸酰氯、十二烷酰氯(月桂酰氯)、椰油酰氯(椰子油衍生的脂肪酸氯化物)、十四烷酰氯(肉豆蔻酰氯)、十六烷酰氯(棕榈酰氯)、十八烷酰氯(硬脂酰氯)、9-十八碳烯酰氯(油酰氯)、二十烷酰氯(花生酰氯)、二十二烷酰氯(山萮酰氯)及其任何混合物的氯化酰基。其他卤化酰基包括前述脂肪酸的溴化物、氟化物和碘化物。制备卤化酰基的方法以及酰化氨基酸的替代方法在2008年8月21日公布的美国专利申请公开号2008/0200704中阐述,该申请通过引用并入本文。
在一个实施方案中,所述氨基酸表面活性剂由式(I)表示:
其中:
Z表示具有8至22个碳原子的饱和或不饱和、直链或支链的烃基,
X是氢或甲基,
n是0或1,
Y选自氢、-CH3、-CH(CH3)2、-CH2CH(CH3)2、-CH(CH3)CH2CH3、-CH2C6H5、-CH2C2H4OH、-CH2OH、-CH(OH)CH3、-(CH2)4NH2、-(CH2)3NHC(NH)NH2、-CH2C(O)O-M+、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,并且
M是成盐阳离子,其中COO是抗衡阴离子,例如钠、钾、铵或三乙醇胺。
因此,根据本发明,氨基酸表面活性剂由式(I)表示,
其中:
Z表示具有8至22个碳原子的饱和或不饱和、直链或支链的烃基,
X是氢或甲基,
n是0或1,
Y选自氢、-CH3、-CH(CH3)2、-CH2CH(CH3)2、-CH(CH3)CH2CH3、-CH2C6H5、-CH2C2H4OH、-CH2OH、-CH(OH)CH3、-(CH2)4NH2、-(CH2)3NHC(NH)NH2、-CH2C(O)O-M+、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,并且
M是成盐阳离子,其中COO是抗衡阴离子,例如钠、钾、铵或三乙醇胺。
在一个实施方案中,在式(I)中:
Z表示饱和或不饱和、直链或支链的C8至C22烷基,
X是氢或甲基,
n是0,
Y选自氢、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,和
M是成盐阳离子,其中COO是抗衡阴离子,例如钠、钾、铵或三乙醇胺。
根据本发明的优选实施方案,在式(I)的氨基脂肪酸中:
Z表示饱和或不饱和、直链或支链的C8至C22烷基,
X是氢或甲基,
n是0,
Y选自氢、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,和
M是成盐阳离子,其中COO是抗衡阴离子,例如钠、钾、铵或三乙醇胺。
氨基酸表面活性剂的实例是丙氨酸、精氨酸、天冬氨酸、谷氨酸、甘氨酸、异亮氨酸、亮氨酸、赖氨酸、苯丙氨酸、丝氨酸、酪氨酸、缬氨酸、肌氨酸及其任何混合物的盐。
更特别地,可以提及的氨基酸表面活性剂是例如辛酰谷氨酸二钾、十一碳烯酰谷氨酸二钾、辛酰谷氨酸二钠、椰油酰谷氨酸二钠、月桂酰谷氨酸二钠、硬脂酰谷氨酸二钠、十一碳烯酰谷氨酸二钠、辛酰谷氨酸钾、椰油酰谷氨酸钾、月桂酰谷氨酸钾、肉豆蔻酰谷氨酸钾、硬脂酰谷氨酸钾、十一碳烯酰谷氨酸钾、辛酰谷氨酸钠、椰油酰谷氨酸钠、月桂酰谷氨酸钠、肉豆蔻酰谷氨酸钠、橄榄油酰谷氨酸钠、棕榈酰谷氨酸钠、硬脂酰谷氨酸钠、十一碳烯酰谷氨酸钠、椰油酰基甲基β-丙氨酸盐、月桂酰基β-丙氨酸盐、月桂酰基甲基β-丙氨酸盐、肉豆蔻酰基β-丙氨酸盐、月桂酰基甲基β-丙氨酸钾、椰油酰丙氨酸钠、椰油酰基甲基β-丙氨酸钠和肉豆蔻酰基甲基β-丙氨酸钠棕榈酰甘氨酸盐、月桂酰甘氨酸钠、椰油酰甘氨酸钠、肉豆蔻酰甘氨酸钠、月桂酰甘氨酸钾、椰油酰甘氨酸钾、月桂酰肌氨酸钾、椰油酰肌氨酸钾、椰油酰肌氨酸钠、月桂酰肌氨酸钠、肉豆蔻酰肌氨酸钠、油酰肌氨酸钠、棕榈酰肌氨酸钠月桂酰肌氨酸铵、月桂酰天冬氨酸钠、肉豆蔻酰天冬氨酸钠、椰油酰天冬氨酸钠、己酰天冬氨酸钠、月桂酰天冬氨酸二钠、肉豆蔻酰天冬氨酸二钠、椰油酰天冬氨酸二钠、己酰天冬氨酸二钠、月桂酰天冬氨酸钾、肉豆蔻酰天冬氨酸钾、椰油酰天冬氨酸钾、己酰天冬氨酸钾、月桂酰天冬氨酸二钾、肉豆蔻酰天冬氨酸二钾、椰油酰天冬氨酸二钾、己酰天冬氨酸二钾及其混合物。
可以参考的可商购获得的氨基酸表面活性剂是例如酰基肌氨酸盐,例如由Ciba公司以名称Sarkosyl NL 销售的月桂酰肌氨酸钠或由SEPPIC公司以名称Oramix L 销售的月桂酰肌氨酸钠,由Nikkol公司以名称Nikkol Sarcosinate 销售的肉豆蔻酰肌氨酸钠或由Nikkol公司以名称Nikkol Sarcosinate 销售的棕榈酰肌氨酸钠,或其混合物。
可以提及的组合物中的可商购获得的优选氨基酸表面活性剂是月桂酰肌氨酸钠(由Seppic销售的ORAMIX L 30)。
优选地,相对于组合物的总重量,氨基脂肪酸表面活性剂以0.1重量%至20重量%,优选0.5重量%至15重量%,更优选1重量%至10重量%的范围内的量存在于组合物中。
两性或两性离子表面活性剂
可以用于本发明的两性或两性离子表面活性剂可以是含有至少一个阴离子基团例如羧酸根、磺酸根、硫酸根、磷酸根或膦酸根的季铵化脂族仲胺或叔胺衍生物,并且其中脂族基团或至少一个脂族基团是包含8至22个碳原子的直链或支链。
尤其可以提及(C8-C20)烷基甜菜碱、磺基甜菜碱、(C8-C20烷基)酰氨基(C2-C8烷基)甜菜碱和(C8-C20烷基)酰氨基(C2-C8烷基)磺基甜菜碱。
在(C8-C20)烷基甜菜碱中,可以提及山萮基甜菜碱、鲸蜡基甜菜碱、椰油基甜菜碱、癸基甜菜碱。从烷基甜菜碱中,椰油基甜菜碱是优选的,例如由Rhodia公司以商品名BB/FLA销售的产品。
在可以使用的任选季铵化脂族仲胺或叔胺衍生物中,还可以提及分别具有以下结构(A1)和(A2)的产品:
(A1)Ra-CON(Z)CH2-(CH2)m-N+(Rb)(Rc)(CH2COO-)
其中:
Ra表示优选存在于水解椰子油中的衍生自酸Ra-COOH的C10-C30烷基或烯基,庚基,壬基或十一烷基,
Rb表示β-羟乙基,
Rc表示羧甲基;
m等于0、1或2,
Z表示氢原子或羟乙基或羧甲基;
(A2)Ra’-CON(Z)CH2-(CH2)m’-N(B)(B')
其中:
B表示-CH2CH2OX',其中X'表示-CH2-COOH、CH2-COOZ’、-CH2CH2-COOH、-CH2CH2-COOZ’,或氢原子,
B'表示-(CH2)z-Y',其中z=1或2,并且Y'表示-COOH、-COOZ’、-CH2-CHOH-SO3H或-CH2-CHOH-SO3Z’,
m'等于0、1或2,
Z表示氢原子或羟乙基或羧甲基,
Z'表示由碱金属或碱土金属如钠、钾或镁产生的离子;铵离子;或由有机胺且特别是由氨基醇如单乙醇胺、二乙醇胺和三乙醇胺、单异丙醇胺、二异丙醇胺或三异丙醇胺、2-氨基-2-甲基-1-丙醇、2-氨基-2-甲基-1,3-丙二醇和三(羟甲基)氨基甲烷产生的离子,
Ra'表示优选存在于水解亚麻子油或椰子油中的酸Ra'COOH的C10-C30烷基或烯基,烷基,特别是C17烷基及其异构形式或不饱和C17基团。
对应于式(A1)的化合物是优选的。
在对应于式(A1)的化合物中,可以提及椰油酰胺丙基甜菜碱,例如由Cognis(BASF)以商品名Dehyton PK 45销售的产品。
也可以使用式(A3)的化合物:
(A3)Ra”-NH-CH(Y”)-(CH2)n-C(O)-NH-(CH2)n’-N(Rd)(Re)
其中:
-Ra”表示优选存在于水解亚麻子油或椰子油中的酸Ra”-C(O)OH的C10-C30烷基或烯基;
-Y”表示基团-C(O)OH、-C(O)OZ”、-CH2-CH(OH)-SO3H或基团-CH2-CH(OH)-SO3-Z”,其中Z”表示由碱金属或碱土金属如钠产生的阳离子抗衡离子,铵离子或由有机胺产生的离子;
-Rd和Re彼此独立地表示C1-C4烷基或羟烷基;和
-n和n’彼此独立地表示1至3范围内的整数。
在对应于式(A3)的化合物中,尤其可以提及以名称二乙氨基丙基椰油基天冬氨酰胺钠分类在CTFA字典中的化合物,例如由Chimex公司以名称Chimexane HB销售的化合物。
优选地,两性表面活性剂选自(C8-C20)烷基甜菜碱、(C8-C20)烷基酰氨基(C1-C6)烷基甜菜碱及其混合物。
更优选地,两性或两性离子表面活性剂选自椰油酰胺丙基甜菜碱、椰油基甜菜碱或其混合物。
有利地,相对于组合物的总重量,两性或两性离子表面活性剂以0.5重量%至20重量%,优选1重量%至15重量%范围内的量存在于组合物中。
固体脂肪酸
本发明的组合物包含至少一种固体脂肪酸。
术语“脂肪醇”是指包含10至40个碳原子,优选12至30个碳原子并且包含至少一个基团COOH的长链脂族醇。这些脂肪酸既不是氧化烯化也不是甘油化的。
“固体脂肪酸”在室温(25℃)和大气压(760mmHg或1个大气压)下为固体;它们是不溶于水的,即它们在水中具有小于1质量%,且优选小于0.5重量%的溶解度。
优选地,固体脂肪酸具有结构R-COOH,其中R表示饱和或不饱和的直链烷基,其任选被一个或多个羟基取代,其包含12至30个碳原子。
优选地,用于本发明的固体脂肪酸选自具有12至20个碳原子的脂肪酸。
作为固体脂肪酸,可以提及癸酸、月桂酸、肉豆蔻酸、肉豆蔻烯酸、棕榈酸、棕榈油酸、顺式6-十六碳烯酸(sapienic acid)、硬脂酸、油酸、反油酸、异油酸、亚油酸、α-亚麻酸、花生酸、花生四烯酸、二十碳五烯酸、山萮酸、芥酸、二十二碳六烯酸、木蜡酸、蜡酸或其混合物。
更优选地,根据本发明,固体脂肪酸选自具有12至20个碳原子的直链饱和脂肪酸,如月桂酸,肉豆蔻酸,棕榈酸,硬脂酸,花生酸或其混合物。
更特别地,固体脂肪酸选自月桂酸,肉豆蔻酸,棕榈酸,硬脂酸或其混合物。
脂肪酸可以是混合物,这意味着例如几种物质可以以混合物的形式共存于商业产品中,尤其是具有不同链长的。
可以提及的这种脂肪醇混合物是月桂酸,其可以从Pacific Oleochemicals公司以商品名Kortacid 1299商购获得。
根据一个实施方案,相对于组合物的总重量,固体脂肪酸以0.1重量%至10重量%,优选0.5重量%至5重量%的范围内的量存在于组合物中。
淀粉磷酸酯
本发明的组合物包含至少一种淀粉磷酸酯或其混合物。
可用于本发明的淀粉磷酸酯更特别是由葡糖酐单元的基本(elemental)单元形成的聚合物形式的大分子。这些单元的数量和它们的组合使得可以区分直链淀粉(直链聚合物)和支链淀粉(支链聚合物)。直链淀粉和支链淀粉的相对比例及其聚合度随淀粉的植物来源而变化。
用于本发明的淀粉分子可以源自植物源,例如谷类、块茎、根、豆类和水果。因此,淀粉可以源自选自玉米、豌豆、马铃薯、甘薯、香蕉、大麦、小麦、大米、燕麦、西米、木薯和高粱的植物源。淀粉优选来源于玉米。
也可以使用上述淀粉水解产物。
淀粉磷酸酯通常呈白色粉末的形式,其基本粒度在3至100微米的范围内。
本发明的组合物中使用的淀粉可以通过以下反应中的一种或多种进行化学改性:预糊化、氧化、交联、酯化、热处理。
特别地,交联反应是优选的。该反应通过与能够与淀粉分子的羟基反应的官能剂交联来进行,所述淀粉分子因此将结合在一起(例如与甘油基和/或磷酸根结合)。
更特别地,淀粉磷酸酯选自:
-式(II)的单淀粉磷酸酯,
Am-O-PO-(OX)2(II),
-式(III)的二淀粉磷酸酯,
Am-O-PO-(OX)-O-Am(III),
-式(IV)的三淀粉磷酸酯,
Am-O-PO-(O-Am)2(IV)
-或其混合物,
其中:
Am是指淀粉;
X表示碱金属(例如钠或钾),碱土金属(例如钙或镁),铵盐,胺盐,例如单乙醇胺、二乙醇胺、三乙醇胺、3-氨基-1,2-丙二醇的那些,或衍生自碱性氨基酸如赖氨酸、精氨酸、肌氨酸、鸟氨酸或瓜氨酸的铵盐。
优选地,本发明的淀粉磷酸酯选自上述式(III)的二淀粉磷酸酯。
可以提及的二淀粉磷酸酯是例如由Avebe公司以参考Prejel VA-70-T AGGL(糊化羟丙基木薯二淀粉磷酸酯)、Prejel TK1(糊化木薯二淀粉磷酸酯)和Prejel 200(糊化乙酰基木薯二淀粉磷酸酯)销售的产品,或由Akzo Nobel公司以参考Structure Zea(糊化羟丙基玉米二淀粉磷酸酯)销售的产品。
优选地,相对于组合物的总重量,淀粉磷酸酯以0.05至10重量%,优选0.1至7重量%,且还更好地0.5至5重量%范围内的量存在于本发明的组合物中。
丙烯酸类增稠聚合物
本发明的组合物包含至少一种丙烯酸类增稠聚合物。
为了本发明的目的,术语“丙烯酸类聚合物”是指由至少一种或多种具有以下结构的单体聚合产生的聚合物:
R3表示氢原子或直链或支链的C1-C4烷基,
R4表示氢原子,直链或支链的C1-C4烷基,基团NR5R6或直链或支链的C1-C30烷氧基,任选被一个或多个羟基或被季铵基取代,
R5和R6表示氢原子或任选氧化烯化的C1-C30烷基,所述烷基可能包含磺酸基。
优选地,R3表示氢原子或甲基。
为了本发明的目的,术语“增稠聚合物”是指这种聚合物,作为在25℃下在水中或乙醇中的1重量%的活性物质溶液或分散体,其在1s-1的剪切速率下具有大于0.2泊的粘度。用来自Thermo Electron的Haake RS600粘度计测量粘度。该粘度计是具有锥板几何形状(例如直径60mm)的受控应力粘度计。
增稠聚合物特别地选自:
(a)丙烯酸类缔合聚合物;
(b)交联丙烯酸均聚物;
(c)(甲基)丙烯酸和丙烯酸(C1-C6)烷基酯的交联共聚物;
(d)含有酯和/或酰胺型烯属不饱和单体的非离子均聚物和共聚物;
(e)丙烯酸铵均聚物或丙烯酸铵与丙烯酰胺的共聚物;
(f)(甲基)丙烯酰氨基(C1-C4)烷基磺酸均聚物和共聚物;
(g)交联的甲基丙烯酰基(C1-C4)烷基三(C1-C4)烷基铵均聚物和共聚物。
根据本发明,表述“缔合聚合物”是指包含至少一个脂肪链,即疏水部分和至少一个亲水部分的两亲聚合物。
与聚合物链的其余部分相比,疏水部分的数量可以更小,并且可以位于侧链并以无规方式分布(无规共聚物)或以嵌段或接枝的形式分布(嵌段共聚物或序列共聚物)。
可以使用水溶性聚合物或水分散性聚合物。优选地,用于本发明的两亲聚合物不交联。
本发明的缔合聚合物是阴离子型并且包含至少一种不饱和羧酸作为单体。可用于本发明聚合物中的不饱和羧酸优选选自丙烯酸、甲基丙烯酸、巴豆酸、衣康酸和马来酸。
如本发明中使用的表述“脂肪链”是指含有8至30个碳原子的直链或支链烃基。
优选地,根据一个实施方案,本发明的丙烯酸类增稠聚合物选自丙烯酸类缔合聚合物,(甲基)丙烯酸和丙烯酸(C1-C6)烷基酯的交联共聚物,或其混合物。
可以根据本发明使用的丙烯酸类缔合聚合物(a)是选自以下的丙烯酸类缔合聚合物:包含至少一个脂肪链和至少一个亲水单元的非离子两亲聚合物;包含至少一个亲水单元和至少一个脂肪链单元的阴离子型两亲聚合物;包含至少一个亲水单元和/或至少一个脂肪链单元的阳离子型两亲聚合物;包含至少一个亲水单元和至少一个脂肪链单元的两性两亲聚合物;含有10至30个碳原子的脂肪链;或其混合物。
优选地,丙烯酸类缔合聚合物选自包含至少一个亲水单元和至少一个脂肪链单元的阴离子型两亲聚合物。
可以引用本发明的以下阴离子型丙烯酸类缔合聚合物:
·包含至少一个亲水基元和至少一个脂肪链烯丙基醚基元的共聚物,其亲水基元由乙烯基羧酸构成,并且更特别地由丙烯酸或甲基丙烯酸或其混合物构成,并且其脂肪链烯丙基醚基元对应于具有下式(V)的单体:
CH2=C R’CH2 O Bn R(V)
其中:
R'表示H或CH3;
B表示乙烯氧基;
n是零或表示1至100的整数;
R表示选自含有8至30个碳原子,优选10至24个,且更特别是12至18个碳原子的烷基、芳基烷基、芳基、烷基芳基和环烷基的烃基。
具有式(V)的更特别优选的基元是其中R'表示H,n等于10且R表示硬脂基(C18)的基元。
这种类型的阴离子型缔合聚合物已被描述并通过专利EP-A-0216479中的乳液聚合方法制备。
本发明特别优选的聚合物包括由20重量%至60重量%的丙烯酸和/或甲基丙烯酸,5重量%至60重量%的(甲基)丙烯酸低级烷基酯,2重量%至50重量%的具有式(V)的脂肪链烯丙基醚和0至1重量%的交联剂形成的聚合物,所述交联剂为熟知的可共聚不饱和聚乙烯属(polyethylenic)单体,例如邻苯二甲酸二烯丙酯,(甲基)丙烯酸烯丙酯,二乙烯基苯,(聚)乙二醇二甲基丙烯酸酯或亚甲基双丙烯酰胺。
在这些后者中,以下是特别优选的:由ALLIED COLLOIDS以商品名SALCARE SC 和SALCARE SC 销售的交联三元共聚物,它们是甲基丙烯酸、丙烯酸乙酯和硬脂醇聚醚-10烯丙基醚(40/50/10)的交联三元共聚物的30%水乳液。
还可以引用由ALLIED COLLOIDS提出的产品RHOEVIS-CR、-CR3和-CRX作为该产品类别中的聚合物;
·甲基丙烯酸/丙烯酸烷基酯/聚氧乙烯化丙烯酸月桂酯三元共聚物,例如由COATEX销售的RHEO 2000;
·甲基丙烯酸/丙烯酸烷基酯/聚氧乙烯化甲基丙烯酸十八烷醇酯共聚物,例如由ROHM&HAAS销售的ACRYSOL 22(或ACULYN 22或ACRYSOL ICS),ACRYSOL 25和DW-1206A;
·甲基丙烯酸/丙烯酸烷基酯/聚氧乙烯化壬基苯酚丙烯酸酯共聚物,例如由COATEX销售的RHEO 3000;
·甲基丙烯酸/丙烯酸丁酯/包含脂肪链的疏水单体共聚物,例如由NATIONALSTARCH销售的8069-146A产品;
·包含至少一种不饱和烯属羧酸类型的亲水基元和至少一种不饱和羧酸类型的C10-C30烷基酯的疏水基元的共聚物。
优选的缔合聚合物如下:
·丙烯酸/乙基C1-C8丙烯酸酯/甲基丙烯酸十八烷醇酯聚氧乙烯化,例如使用20摩尔的环氧乙烷,例如由ROHM&HAAS以商品名“ACRYSOL ICS或ACRYSOL ZZ或ACULYN 22”销售的产品。
取决于它们的性质,本发明的缔合聚合物可以以水溶液的形式或以水分散体的形式使用。
在(甲基)丙烯酸和丙烯酸C1-C6烷基酯的交联共聚物(c)中可以提及的是由Coatex公司以名称Viscoatex 538C销售的产品,其是作为含有38%活性物质的水分散体的甲基丙烯酸和丙烯酸乙酯的交联共聚物,或由Rohm&Haas公司以名称Aculyn 33销售的产品,其是作为含有28%活性物质的水分散体的丙烯酸和丙烯酸乙酯的交联共聚物。将更特别地提及由Noveon公司制造和以名称Carbopol Aqua SF-1销售的呈30%水分散体形式的交联甲基丙烯酸/丙烯酸乙酯共聚物。
优选地,在(甲基)丙烯酸和丙烯酸C1-C6烷基酯的交联共聚物(c)中可以提及,使用丙烯酸和丙烯酸乙酯的交联共聚物。
根据优选的实施方案,相对于组合物的总重量,丙烯酸类增稠聚合物以0.1重量%至10重量%,优选0.5重量%至5重量%范围内的量存在于组合物中。
有利地,本发明涉及用于清洁角蛋白材料的组合物,其包含相对于组合物的总重量:
A)0.5重量%至15重量%的至少一种式(I)的氨基酸表面活性剂,
其中:
Z表示饱和或不饱和、直链或支链的C8-C22烷基,
X是氢或甲基,
n是0,
Y选自氢、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,和
M是成盐阳离子,其中COO是抗衡阴离子,例如钠、钾、铵或三乙醇胺,
B)1重量%至15重量%的至少一种选自(C8-C20)烷基甜菜碱、(C8-C20)烷基酰氨基(C1-C6)烷基甜菜碱及其混合物的两性或两性离子表面活性剂;
C)0.5重量%至5重量%的至少一种具有12至20个碳原子的固体脂肪酸;
D)0.1重量%至7重量%的至少一种式(III)的二淀粉磷酸酯,
Am-O-PO-(OX)-O-Am(III),
其中:
Am是指淀粉;
X表示碱金属、铵盐、胺盐或衍生自碱性氨基酸的铵盐;和
E)0.5重量%至5重量%的至少一种选自丙烯酸类缔合聚合物、(甲基)丙烯酸和丙烯酸(C1-C6)烷基酯的交联共聚物,或其混合物的丙烯酸类增稠聚合物。
方法和用途
本发明的组合物可以通过施用于角蛋白材料而用于清洁角蛋白材料例如皮肤和头皮,特别是面部的方法。
特别地,所述方法包括在任选的一段时间后用水冲洗掉本发明的组合物。
本发明还涉及根据本发明的组合物用于清洁角蛋白材料,特别是针对皮肤和头皮,并且更特别是针对面部的用途。
本发明涉及用于清洁角蛋白材料的方法,该方法包括将至少一种本发明的组合物施用于所述角蛋白材料的表面,其中所述角蛋白材料优选为皮肤和头皮,特别是面部。
以下实施例旨在例示根据本发明的组合物和方法,但不以任何方式限制本发明的范围。
实施例
实施例1:配制实施例
制备了以下配制物:
比较配制物B含有除本发明所要求保护的聚合物之外的聚合物。
配制物通过如下制备:混合相A并加热至75℃,将相B添加至相A(70℃)并混合5分钟,将相C添加至相A与相B的混合物(65℃)并混合5分钟,然后向上述获得的混合物在65℃下分别添加相D和E并混合10分钟。
用于混合的机器是由i-Tech公司销售的均化器VMI。
根据本发明的面部清洁剂C和比较清洁剂D被制备:
比较清洁剂D含有阴离子型表面活性剂,而不是如本发明中所要求保护的氨基酸表面活性剂。
上述面部清洁剂按以下步骤制备:
混合相A,将其加热至75℃,
在75℃下将相B加入相A并混合5分钟,
在70℃下添加相C并混合5分钟;
在65℃下添加预相D并混合5分钟;
在65℃下添加相E并混合10分钟;
在65℃下添加相F并混合10分钟;
在50℃下添加相G;
在40℃以下添加预相H和I。
用于混合的机器是由i-Tech公司销售的均化器VMI。
实施例2:评价实施例
5名消费者通过使用本发明和比较配制物作为面部清洁剂来评价本发明和比较配制物的冲洗速度以及泡沫密度。
在5名女性消费者的面部上分别施用0.5g的本发明和比较配制物,并且由消费者按摩带配制物的面部X分钟。然后用温水冲洗面部。10分钟后,就以下效果给出分数:
冲洗速度:在皮肤上不存在粘滑感时的时间段,这表示面部被冲洗且是清洁的;它由循环数表示。循环数越少,冲洗速度越快。
用“循环”旨在表示使用手冲洗面部皮肤的动作,特别是使用手指通过在面颊上或从前额到面颊底部转动来洗涤面部皮肤。
泡沫密度:泡沫密度由消费者在按摩面部时进行评价,其中分别施用本发明和比较配制物。更特别地,消费者在施用配制物期间通过在手和面部皮肤之间按压泡沫,在分别施用了本发明和比较配制物的面部皮肤的40轮摩擦之后评价泡沫密度。
消费者给出1至15分的泡沫密度。给出的分数越高,配制物的泡沫密度越好。通过在4℃、20℃、40℃和45℃下储存配制物2个月来评价本发明和比较配制物的稳定性。
结果如下:
从上面列出的结果可以看出,与比较配制物B相比,本发明配制物A和C显示出好得多的冲洗速度,良好的稳定性以及改进的泡沫密度。
此外,在皮脂存在下,对清洁剂C和D的发泡体积进行评价。
将14.2g的清洁剂C和D分别加入到85.3g的水中,并分别在两种混合物中加入0.5g的模拟皮脂。
然后使用Philips Blender(HR2024,220V,50Hz,400W),使用齿轮1将混合物共混20秒。
在1000ml量筒中测量共混步骤期间产生的泡沫。最后,记录泡沫体积。
模拟皮脂由0.14g肉豆蔻酸、0.25g甘油三酸酯(tryglyceride)和0.11g角鲨烯组成。模拟皮脂是模拟面部皮肤上产生的皮脂。
结果如下:
清洁剂 | 发泡体积(ml) |
C | 370 |
D | 225 |
可以看到,与含有较高量的阴离子型表面活性剂的因其发泡性能而众所周知的比较清洁剂D相比,用较少量的表面活性剂,本发明面部清洁剂C呈现好得多的发泡体积。
Claims (22)
1.一种组合物,其包含:
a)至少一种氨基酸表面活性剂;
b)至少一种两性或两性离子表面活性剂;
c)至少一种固体脂肪酸;
d)至少一种淀粉磷酸酯;和
e)至少一种选自(甲基)丙烯酸和丙烯酸(C1-C6)烷基酯的交联共聚物的丙烯酸类增稠聚合物。
2.权利要求1所述的组合物,其中所述氨基酸表面活性剂选自式(I)的化合物,
其中在式(I)中:
Z表示具有8至22个碳原子的饱和或不饱和、直链或支链的烃基,
X是氢或甲基,
n是0或1,
Y选自氢、-CH3、-CH(CH3)2、-CH2CH(CH3)2、-CH(CH3)CH2CH3、-CH2C6H5、-CH2C2H4OH、-CH2OH、-CH(OH)CH3、-(CH2)4NH2、-(CH2)3NHC(NH)NH2、-CH2C(O)O-M+、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,并且
M是成盐阳离子,其中COO是抗衡阴离子。
3.权利要求2所述的组合物,其中在式(I)中:
Z表示饱和或不饱和、直链或支链的C8至C22烷基,
X是氢或甲基,
n是0,
Y选自氢、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,和
M是成盐阳离子,其中COO是抗衡阴离子。
4.权利要求2或3所述的组合物,其中M是钠、钾、铵或三乙醇胺。
5.权利要求1或2所述的组合物,其中所述氨基酸表面活性剂选自酰基肌氨酸盐。
6.权利要求5所述的组合物,其中所述氨基酸表面活性剂选自月桂酰肌氨酸钠、肉豆蔻酰肌氨酸钠、棕榈酰肌氨酸钠,或其混合物。
7.前述权利要求1至2中任一项所述的组合物,其中相对于所述组合物的总重量,所述氨基脂肪酸表面活性剂以在0.1重量%至20重量%的范围内的量存在于所述组合物中。
8.前述权利要求1至2中任一项所述的组合物,其中所述两性或两性离子表面活性剂选自(C8-C20)烷基甜菜碱、(C8-C20)烷基酰氨基(C1-C6)烷基甜菜碱及其混合物。
9.权利要求8所述的组合物,其中所述两性或两性离子表面活性剂选自椰油酰胺丙基甜菜碱、椰油基甜菜碱或其混合物。
10.前述权利要求1至2中任一项所述的组合物,其中相对于所述组合物的总重量,所述两性或两性离子表面活性剂以在0.5重量%至20重量%的范围内的量存在于所述组合物中。
11.前述权利要求1至2中任一项所述的组合物,其中所述固体脂肪酸选自具有12至20个碳原子的脂肪酸。
12.权利要求11所述的组合物,其中所述固体脂肪酸选自月桂酸、肉豆蔻酸、棕榈酸、硬脂酸、花生酸或其混合物。
13.前述权利要求1至2中任一项所述的组合物,其中相对于所述组合物的总重量,所述固体脂肪酸以在0.1重量%至10重量%的范围内的量存在于所述组合物中。
14.前述权利要求1至2中任一项所述的组合物,其中所述淀粉磷酸酯选自:
-式(II)的单淀粉磷酸酯,
Am-O-PO-(OX)2(II),
-式(III)的二淀粉磷酸酯,
Am-O-PO-(OX)-O-Am(III),
-式(IV)的三淀粉磷酸酯,
Am-O-PO-(O-Am)2(IV)
或其混合物,
其中:
Am是指淀粉;
X代表碱金属、铵盐、胺盐或衍生自碱性氨基酸的铵盐。
15.前述权利要求1至2中任一项所述的组合物,其中所述淀粉磷酸酯选自式(II)的二淀粉磷酸酯。
16.权利要求15所述的组合物,其中所述淀粉磷酸酯选自糊化羟丙基木薯二淀粉磷酸酯、糊化乙酰木薯二淀粉磷酸酯、糊化羟丙基玉米二淀粉磷酸酯或其混合物。
17.前述权利要求1至2中任一项所述的组合物,其中相对于所述组合物的总重量,所述淀粉磷酸酯以在0.05重量%至10重量%的范围内的量存在于所述组合物中。
18.前述权利要求1至2中任一项所述的组合物,其中所述丙烯酸类增稠聚合物是丙烯酸和丙烯酸乙酯的交联共聚物。
19.前述权利要求1至2中任一项所述的组合物,其中相对于所述组合物的总重量,所述丙烯酸类增稠聚合物以在0.1重量%至10重量%的范围内的量存在于所述组合物中。
20.用于清洁角蛋白材料的组合物,其包含相对于所述组合物的总重量:
A)0.5重量%至15重量%的至少一种式(I)的氨基酸表面活性剂,
其中:
Z表示饱和或不饱和、直链或支链的C8-C22烷基,
X是氢或甲基,
n是0,
Y选自氢、-(CH2)2C(O)OH、-(CH2)2C(O)O-M+,和
M是成盐阳离子,其中COO是抗衡阴离子,
B)1重量%至15重量%的至少一种选自(C8-C20)烷基甜菜碱、(C8-C20)烷基酰氨基(C1-C6)烷基甜菜碱及其混合物的两性或两性离子表面活性剂;
C)0.5重量%至5重量%的至少一种具有12至20个碳原子的固体脂肪酸;
D)0.1重量%至7重量%的至少一种式(III)的二淀粉磷酸酯,
Am-O-PO-(OX)-O-Am(III),
其中:
Am是指淀粉;
X表示碱金属、铵盐、胺盐或衍生自碱性氨基酸的铵盐;和
E)0.5重量%至5重量%的至少一种选自(甲基)丙烯酸和丙烯酸(C1-C6)烷基酯的交联共聚物的丙烯酸类增稠聚合物。
21.一种通过向角蛋白材料施用前述权利要求1至20中任一项所述的组合物来清洁角蛋白材料的方法。
22.根据前述权利要求1至20中任一项所述的组合物用于清洁角蛋白材料的用途。
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- 2015-12-10 WO PCT/CN2015/097003 patent/WO2017096587A1/en active Application Filing
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JP2018534369A (ja) | 2018-11-22 |
EP3386475A4 (en) | 2019-07-10 |
WO2017096587A1 (en) | 2017-06-15 |
US20180333344A1 (en) | 2018-11-22 |
EP3386475B1 (en) | 2022-08-31 |
BR112018006435A2 (pt) | 2019-04-30 |
BR112018006435B1 (pt) | 2021-02-02 |
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EP3386475A1 (en) | 2018-10-17 |
JP6728378B2 (ja) | 2020-07-22 |
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